Asunto(s)
Enfermedades de las Arterias Carótidas/etiología , Infección Focal Dental/complicaciones , Hemorragia/etiología , Mediastinitis/complicaciones , Enfermedades de las Arterias Carótidas/diagnóstico , Enfermedades de las Arterias Carótidas/terapia , Arteria Carótida Interna/cirugía , Terapia Combinada , Urgencias Médicas , Infección Focal Dental/diagnóstico , Infección Focal Dental/terapia , Hemorragia/diagnóstico , Hemorragia/terapia , Humanos , Ligadura , Masculino , Mediastinitis/diagnóstico , Mediastinitis/etiología , Mediastinitis/terapia , Persona de Mediana Edad , ReoperaciónAsunto(s)
Carcinoma Krebs 2/patología , Ciclofosfamida/farmacología , Ultrasonido , Animales , División Celular/efectos de los fármacos , Permeabilidad de la Membrana Celular/efectos de los fármacos , Resistencia a Medicamentos , Espectroscopía de Resonancia por Spin del Electrón , Radicales Libres , Peroxidación de Lípido , Ratones , Marcadores de Spin , Células Tumorales Cultivadas/efectos de los fármacosRESUMEN
BACKGROUND: Tracer studies are an important tool to obtain information about the processes involved in the immunological response. Colloidal gold is widely used as a tracer, but its small size of label can cause some difficulty during low-resolution analysis. To overcome this difficulty, we developed a new method to follow the route of tracer movement within lymph nodes. METHODS: We applied conventional X-ray analysis, X-ray fluorescence analysis (XFA) subtractional microscopy using synchrotron radiation (SR) beams, light microscopy, and ultrastructural analysis to study the distribution and quantity of colloidal gold coupled with albumin within rat parasternal lymph node 2, 4, 6, 8, and 10 h after intrapleural injection of the tracer. RESULTS: At all the time points XFA-SR revealed that tracer formed a circle with a maximum concentration in the node periphery. XFA-SR measured colloidal gold concentration in the nodes reached its maximum (0.5-0.75 weight %) in 6-8 h. Subtractional microscopy revealed superficially located groups of cells filled with colloidal gold tracer. Light microscopy and ultrastructural analysis confirmed that the tracer was concentrated in the reticular cells, situated in the sinuses of the node. Sinusoidal reticular cells concentrated tracer at much higher rates than sinusoidal macrophages. Four hours after injection, gold appeared in the lysosomes of the follicular reticular cells. At the same time point, evidence of antigen presentation was obtained. Antigen presentation proved to be an extremely rara event since only one ultrastructural incident was found in 150 analysed grids. CONCLUSIONS: SR is a valuable tool for the analysis of gold tracer passage within the living organism.